Product NDC: | 51325-100 |
Proprietary Name: | Rejuvaderm Medispa sunscreen |
Non Proprietary Name: | Octinoxate, Octisalate, Zinc oxide |
Active Ingredient(s): | 9; 2.4; 9 mL/120mL; mL/120mL; mL/120mL & nbsp; Octinoxate, Octisalate, Zinc oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51325-100 |
Labeler Name: | Ellen H Frankle MD Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100801 |
Package NDC: | 51325-100-01 |
Package Description: | 120 mL in 1 TUBE (51325-100-01) |
NDC Code | 51325-100-01 |
Proprietary Name | Rejuvaderm Medispa sunscreen |
Package Description | 120 mL in 1 TUBE (51325-100-01) |
Product NDC | 51325-100 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Octisalate, Zinc oxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20100801 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Ellen H Frankle MD Inc |
Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
Strength Number | 9; 2.4; 9 |
Strength Unit | mL/120mL; mL/120mL; mL/120mL |
Pharmaceutical Classes |